FDA 510(k) Applications Submitted by PEAK SURGICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K102709 |
09/20/2010 |
PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE |
PEAK SURGICAL, INC. |
| K082786 |
09/23/2008 |
PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES |
PEAK SURGICAL, INC. |
| K073057 |
10/30/2007 |
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040 |
PEAK SURGICAL, INC. |
| K102029 |
07/19/2010 |
PEAK PULSAR II GENERATOR MODEL PS100-102 |
PEAK SURGICAL, INC. |
| K083415 |
11/18/2008 |
PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE |
PEAK SURGICAL, INC. |
| K093695 |
11/30/2009 |
PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE |
PEAK SURGICAL, INC. |
| K103775 |
12/27/2010 |
PEAK SUCTION COAGULATOR |
PEAK SURGICAL, INC. |
|
|
